(Q36857266)

English

Deficiency of ATP2C1, a Golgi ion pump, induces secretory pathway defects in endoplasmic reticulum (ER)-associated degradation and sensitivity to ER stress

scientific article published on 28 December 2004

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Deficiency of ATP2C1, a Golgi ion pump, induces secretory pathway defects in endoplasmic reticulum (ER)-associated degradation and sensitivity to ER stress (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

endoplasmic reticulum

0 references

author name string

Jose Ramos-Castañeda

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Young-nam Park

2

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Ming Liu

3

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Karin Hauser

4

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Hans Rudolph

5

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Gary E Shull

6

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Marcel F Jonkman

7

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Kazutoshi Mori

8

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Shigaku Ikeda

9

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Hideoki Ogawa

10

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Peter Arvan

11

1 reference

Europe PubMed Central

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16 August 2017

language of work or name

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publication date

28 December 2004

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Europe PubMed Central

PMC publication ID

16 August 2017

Journal of Biological Chemistry

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Europe PubMed Central

PMC publication ID

16 August 2017

280

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

10

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

9467-9473

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

The expression, activity and localisation of the secretory pathway Ca2+ -ATPase (SPCA1) in different mammalian tissues

1 reference

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Misfolded proteins are sorted by a sequential checkpoint mechanism of ER quality control

1 reference

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Role for plasma membrane-related Ca2+-ATPase-1 (ATP2C1) in pancreatic beta-cell Ca2+ homeostasis revealed by RNA silencing

1 reference

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Cytoprotection by pre-emptive conditional phosphorylation of translation initiation factor 2

1 reference

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Human keratinocyte ATP2C1 localizes to the Golgi and controls Golgi Ca2+ stores

1 reference

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Characterization of Cos-7 cells overexpressing the rat secretory pathway Ca2+-ATPase

1 reference

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The contribution of the SPCA1 Ca2+ pump to the Ca2+ accumulation in the Golgi apparatus of HeLa cells assessed via RNA-mediated interference

1 reference

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Effect of Hailey-Hailey Disease mutations on the function of a new variant of human secretory pathway Ca2+/Mn2+-ATPase (hSPCA1)

1 reference

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BAX and BAK regulation of endoplasmic reticulum Ca2+: a control point for apoptosis

1 reference

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Role of the connecting peptide in insulin biosynthesis

1 reference

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Molecular physiology of the SERCA and SPCA pumps

1 reference

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Two distinctly localized p-type ATPases collaborate to maintain organelle homeostasis required for glycoprotein processing and quality control

1 reference

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The long and short of siRNAs

1 reference

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ER-golgi traffic is a prerequisite for efficient ER degradation.

1 reference

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Cod1p/Spf1p is a P-type ATPase involved in ER function and Ca2+ homeostasis

1 reference

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Dynamic imaging of endoplasmic reticulum Ca2+ concentration in insulin-secreting MIN6 Cells using recombinant targeted cameleons: roles of sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA)-2 and ryanodine receptors

1 reference

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29 September 2017

Functional expression in yeast of the human secretory pathway Ca(2+), Mn(2+)-ATPase defective in Hailey-Hailey disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2527542

29 September 2017

Distinct retrieval and retention mechanisms are required for the quality control of endoplasmic reticulum protein folding

1 reference

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29 September 2017

The KDEL receptor mediates a retrieval mechanism that contributes to quality control at the endoplasmic reticulum

1 reference

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29 September 2017

Response of neurons to an irreversible inhibition of endoplasmic reticulum Ca(2+)-ATPase: relationship between global protein synthesis and expression and translation of individual genes

1 reference

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29 September 2017

Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells

1 reference

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29 September 2017

X-ray crystal structure of rabbit N-acetylglucosaminyltransferase I: catalytic mechanism and a new protein superfamily

1 reference

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29 September 2017

Endoplasmic reticulum (ER)-associated degradation of misfolded N-linked glycoproteins is suppressed upon inhibition of ER mannosidase I.

1 reference

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29 September 2017

The unfolded protein response regulates multiple aspects of secretory and membrane protein biogenesis and endoplasmic reticulum quality control

1 reference

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Perk is essential for translational regulation and cell survival during the unfolded protein response

1 reference

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29 September 2017

A regulatory link between ER-associated protein degradation and the unfolded-protein response

1 reference

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29 September 2017

Calcium, a signaling molecule in the endoplasmic reticulum?

1 reference

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Functional and genomic analyses reveal an essential coordination between the unfolded protein response and ER-associated degradation

1 reference

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29 September 2017

Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2527542

29 September 2017

Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2527542

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Mammalian transcription factor ATF6 is synthesized as a transmembrane protein and activated by proteolysis in response to endoplasmic reticulum stress

1 reference

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The medial-Golgi ion pump Pmr1 supplies the yeast secretory pathway with Ca2+ and Mn2+ required for glycosylation, sorting, and endoplasmic reticulum-associated protein degradation

1 reference

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Apoptosis in insulin-secreting cells. Evidence for the role of intracellular Ca2+ stores and arachidonic acid metabolism

1 reference

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Characterization of a rat liver Golgi sulphotransferase responsible for the 6-O-sulphation of N-acetylglucosamine residues in beta-linkage to mannose: role in assembly of sialyl-galactosyl-N-acetylglucosamine 6-sulphate sequence of N-linked oligosac

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An endoplasmic reticulum storage disease causing congenital goiter with hypothyroidism

1 reference

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Der1, a novel protein specifically required for endoplasmic reticulum degradation in yeast

1 reference

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Mutations in PMR1 suppress oxidative damage in yeast cells lacking superoxide dismutase

1 reference

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Sorting and retrieval between the endoplasmic reticulum and Golgi apparatus

1 reference

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Divalent cation activation of galactosyltransferase in native mammary Golgi vesicles

1 reference

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The endoplasmic reticulum and calcium storage

1 reference

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Regulating the retention of T-cell receptor alpha chain variants within the endoplasmic reticulum: Ca(2+)-dependent association with BiP

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Molecular cloning and tissue distribution of alternatively spliced mRNAs encoding possible mammalian homologues of the yeast secretory pathway calcium pump

1 reference

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The yeast Ca(2+)-ATPase homologue, PMR1, is required for normal Golgi function and localizes in a novel Golgi-like distribution

1 reference

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Endoplasmic reticulum stress proteins block oxidant-induced Ca2+ increases and cell death.

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The endoplasmic reticulum Ca2+ store: a view from the lumen

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The yeast secretory pathway is perturbed by mutations in PMR1, a member of a Ca2+ ATPase family.

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Calcium is required for folding of newly made subunits of the asialoglycoprotein receptor within the endoplasmic reticulum.

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Ca(2+)-ATPases of Saccharomyces cerevisiae: diversity and possible role in protein sorting.

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Desmosome assembly and keratin network formation after Ca2+/serum induction and UVB radiation in Hailey-Hailey keratinocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15623514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Degradation of proteins from the ER of S. cerevisiae requires an intact unfolded protein response pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/15623514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1074/JBC.M413243200

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

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